(Q46391702)

English

Chromosome constitution of 500 infants dying during the perinatal period. With an appendix concerning other genetic disorders among these infants

scientific article

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

Chromosome constitution of 500 infants dying during the perinatal period. With an appendix concerning other genetic disorders among these infants (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

maternal health

0 references

author name string

G A Machin

1

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

J A Crolla

2

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

publication date

1 January 1974

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

language of work

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

23

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

3

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

183-198

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three further cases of triploidy in man surviving to birth

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). 3. FREQUENCY OF INTERCHANGE OF TRISOMICS AND MUTATION RATE OF CHROMOSOME INTERCHANGES

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human population cytogenetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid processing of primary embryonic tissues for chromosome banding pattern analysis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Judgment of fetal age. 3. The pathologist's evaluation

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency and occurrence of chromosomal syndromes: II. E-trisomy

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on chromosomal nondisjunction in man. 3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Post Mortem Chromosome Analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased frequency of chromosomal anomalies in abortions after induced ovulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NECROPSY SPLEEN SAMPLES FOR CHROMOSOME CULTURES

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

THE USE OF THYMUS AND SPLEEN IN THE DEMONSTRATION OF CHROMOSOMES POSTMORTEM IN FOETUSES AND INFANTS

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Survival and the sex ratio in trisomy 17-18

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome aberrations in 2159 consecutive newborn babies

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simple smear method for the sampling and culturing of embryonal and fetal tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CHRONIC FETAL DISTRESS AND PLACENTAL INSUFFICIENCY

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anencephaly and ovulation stimulation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased brain weight-liver weight ratio as a necropsy sign of intrauterine undernutrition

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome studies in 5,049 consecutive newborn children

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome abnormalities in early spontaneous abortions

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome anomalies as a cause of spontaneous abortion

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

E (16-18) trisomy syndrome: analysis of 13 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The endometrial karyotypic profiles of women after clomiphene citrate therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

XYY males in Victoria

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetics of spontaneously aborted human fetuses

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal organ and cellular growth with various chromosomal disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Chromosome aberrations in human spontaneous abortion]

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic analysis of postmortem cultured leukocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome studies in a neonatal population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 17-18. A study of five cases, three of whom were associated with oesophageal atresia

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rapid banding technique for human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Karyotypes of cultured cells from foetal membranes of normal newborns

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Simple Method for Postmortem Cultivation of Human Leucocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anencephaly and ovulation stimulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal anomalies in spontaneously aborted human fetuses

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TRISOMY 18 SYNDROME WITH ABSENT RADIUS, VARUS DEFORMITY OF HAND, AND RUDIMENTARY THUMB: REPORT OF A CASE

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 18, Esophageal Atresia, Anomalies of the Radius, and Congenital Hypoplastic Thrombocytopenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/4844640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00285104

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/4844640

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q46391702&oldid=2109212601"